SRX15234413 GSM6132392_r1 SRP374725 PRJNA837218 SRS12967604 GSM6132392 GSM6132392 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234414 GSM6132393_r1 SRP374725 PRJNA837218 SRS12967605 GSM6132393 GSM6132393 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234415 GSM6132394_r1 SRP374725 PRJNA837218 SRS12967606 GSM6132394 GSM6132394 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234416 GSM6132395_r1 SRP374725 PRJNA837218 SRS12967608 GSM6132395 GSM6132395 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234417 GSM6132396_r1 SRP374725 PRJNA837218 SRS12967607 GSM6132396 GSM6132396 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234418 GSM6132397_r1 SRP374725 PRJNA837218 SRS12967610 GSM6132397 GSM6132397 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234419 GSM6132398_r1 SRP374725 PRJNA837218 SRS12967609 GSM6132398 GSM6132398 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234420 GSM6132399_r1 SRP374725 PRJNA837218 SRS12967612 GSM6132399 GSM6132399 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234421 GSM6132400_r1 SRP374725 PRJNA837218 SRS12967611 GSM6132400 GSM6132400 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234422 GSM6132401_r1 SRP374725 PRJNA837218 SRS12967613 GSM6132401 GSM6132401 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234423 GSM6132402_r1 SRP374725 PRJNA837218 SRS12967614 GSM6132402 GSM6132402 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000 SRX15234424 GSM6132403_r1 SRP374725 PRJNA837218 SRS12967615 GSM6132403 GSM6132403 RNA-Seq TRANSCRIPTOMIC cDNA The RNA was isolated by RNeasy Mini Kit from Qiagen. The integrity of total RNA was examined by the Agilent 4200 TapeStation System. Libraries for RNA-Seq were constructed with Nugen Universal plus mRNA-Seq Kit to generate strand-specific RNA-seq libraries. The workflow consists of poly(A) RNA selection, RNA fragmentation and double-stranded cDNA generation using a mixture of random and oligo(dT) priming, followed by end repair to generate blunt ends, adaptor ligation, strand selection, and PCR amplification to produce the final libraries. Amplified libraries were quantified by Qubit dsDNA HS (High Sensitivity) Assay Kit, and quality-checked by the Agilent 4200 TapeStation System. Different index adaptors were used for multiplexing samples in one sequencing lane. Sequencing was performed with HiSeq3000 sequencer to produce 50 base-pair single-end reads (1 x 50 bp). Illumina HiSeq 3000